An Overview of Microcrystal Electron Diffraction (MicroED)

被引:17
|
作者
Mu, Xuelang [1 ,2 ,3 ]
Gillman, Cody [1 ,2 ,3 ]
Nguyen, Chi [1 ]
Gonen, Tamir [1 ,2 ,3 ]
机构
[1] Univ Calif Los Angeles, Dept Biol Chem, Howard Hughes Med Inst, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Mol Biol Inst, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Howard Hughes Med Inst, Dept Physiol, Los Angeles, CA 90095 USA
基金
美国国家卫生研究院;
关键词
MicroED; microcrystal electron diffraction; cryo-EM; cryo-electron microscopy; structures; crystallography; proteins; CRYO-EM STRUCTURE; CRYOELECTRON MICROSCOPY; RADIATION-DAMAGE; 2-DIMENSIONAL CRYSTALLIZATION; STRUCTURAL BIOLOGY; MEMBRANE-PROTEINS; ATOMIC-RESOLUTION; ALPHA-SYNUCLEIN; DATA-COLLECTION; X-RAYS;
D O I
10.1146/annurev-biochem-081720-020121
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The bedrock of drug discovery and a key tool for understanding cellular function and drug mechanisms of action is the structure determination of chemical compounds, peptides, and proteins. The development of new structure characterization tools, particularly those that fill critical gaps in existing methods, presents important steps forward for structural biology and drug discovery. The emergence of microcrystal electron diffraction (MicroED) expands the application of cryo-electron microscopy to include samples ranging from small molecules and membrane proteins to even large protein complexes using crystals that are one-billionth the size of those required for X-ray crystallography. This review outlines the conception, achievements, and exciting future trajectories for MicroED, an important addition to the existing biophysical toolkit.
引用
收藏
页码:431 / 450
页数:20
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